Simulated microgravity promotes monocyte adhesion to rat aortic endothelium via nuclear factor‐κB activation
- 23 April 2015
- journal article
- Published by Wiley in Clinical and Experimental Pharmacology and Physiology
- Vol. 42 (5) , 510-519
Abstract
Summary: Microgravity‐induced vascular remodelling may play an important role in post‐spaceflight orthostatic intolerance. In this study, we aimed to investigate the effects of simulated microgravity on monocyte adhesion to aortic endothelium in hindlimb unweighted rats and to elucidate the underlying mechanisms associated with this event. Sprague–Dawley rats were subjected to 4‐week hindlimb unweighting to simulate microgravity. The recruitment of monocytes to the abdominal aorta was investigated by en face immunofluorescence staining and monocyte binding assays. The expression of the adhesion molecules E‐selectin and vascular cell adhesion molecule‐1 as well as the cytokine monocyte chemoattractant protein (MCP)‐1 was evaluated by immunohistochemical staining, western blot, and quantitative reverse transcription polymerase chain reaction analyses. Additionally, nuclear factor‐κB (NF‐κB) activation and the messenger RNA expression levels of E‐selectin, vascular cell adhesion molecule‐1, and MCP‐1 were assessed with the administration of an NF‐κB inhibitor, pyrrolidine dithiocarbamate. Results showed that simulated microgravity significantly increased monocyte recruitment to the aortic endothelium, protein expression of E‐selectin and MCP‐1, and NF‐κB activation in the abdominal aorta of rats. Pyrrolidine dithiocarbamate treatment not only significantly inhibited NF‐κB activity but also reduced the messenger RNA levels of E‐selectin, vascular cell adhesion molecule‐1, and MCP‐1 as well as monocyte recruitment in the abdominal aorta of hindlimb unweighted rats. These results suggest that simulated microgravity increases monocyte adhesion to rat aortic endothelium via the NF‐κB‐mediated expression of the adhesion molecule E‐selectin and the cytokine MCP‐1. Therefore, an NF‐κB‐mediated inflammatory response may be one of the cellular mechanisms responsible for arterial remodelling during exposure to microgravity.Keywords
Funding Information
- National Natural Science Foundation of China (30971423)
- National Natural Science Foundation of China (30871218)
- National Natural Science Foundation of China (31070768)
This publication has 27 references indexed in Scilit:
- Spaceflight‐induced alterations in cerebral artery vasoconstrictor, mechanical, and structural properties: implications for elevated cerebral perfusion and intracranial pressureThe FASEB Journal, 2013
- Impairment of Cerebral Blood Flow Regulation in Astronauts With Orthostatic Intolerance After FlightStroke, 2011
- Differential Regulation and Recovery of Intracellular Ca2+ in Cerebral and Small Mesenteric Arterial Smooth Muscle Cells of Simulated Microgravity RatPLOS ONE, 2011
- Inhibition of nuclear factor κB regresses cardiac hypertrophy by modulating the expression of extracellular matrix and adhesion moleculesFree Radical Biology and Medicine, 2011
- A single NFκB system for both canonical and non-canonical signalingCell Research, 2010
- The nuclear factor- B-interleukin-6 signalling pathway mediating vascular inflammationCardiovascular Research, 2010
- Role of nuclear factor κB in cardiovascular health and diseaseClinical Science, 2010
- Contrasting effects of simulated microgravity with and without daily −Gxgravitation on structure and function of cerebral and mesenteric small arteries in ratsJournal of Applied Physiology, 2009
- Inflammatory cytokines in vascular dysfunction and vascular diseaseBiochemical Pharmacology, 2009
- Regional specificity of adaptation change in large elastic arteries of simulated microgravity ratsActa Physiologica Hungarica, 2009